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16506-27-7

16506-27-7 Structure

16506-27-7 Structure
IdentificationBack Directory
[Name]

Bendamustine
[CAS]

16506-27-7
[Synonyms]

Bendamustine
4-(5-(Bis(2-chloroethyl)
-1-methyl-1H-benzo[d]imidazol-2-yl)
5-(Bis(2-chloroethyl)amino)-1-methyl-2-benzimidazolebutyric acid
5-[Bis(2-chloroethyl)amino]-1-methyl-1H-benzimidazole-2-butanoic acid
4-[5-[bis(2-chloroethyl)amino]-1-methylbenzimidazol-2-yl]butanoic acid
1H-BenziMidazole-2-butanoicacid, 5-[bis(2-chloroethyl)aMino]-1-Methyl-
4-(5-(bis(2-chloroethyl)aMino)-1-Methyl-1H-benzo[d]iMidazol-2-yl)butanoic acid
[Molecular Formula]

C16H21Cl2N3O2
[MDL Number]

MFCD00866481
[MOL File]

16506-27-7.mol
[Molecular Weight]

358.26
Chemical PropertiesBack Directory
[Boiling point ]

585.2±50.0 °C(Predicted)
[density ]

1.31±0.1 g/cm3(Predicted)
[storage temp. ]

-20°C, protect from light
[solubility ]

DMSO : 100 mg/mL (279.13 mM; Need ultrasonic)
[form ]

Solid
[pka]

4.50±0.10(Predicted)
[color ]

White to off-white
Safety DataBack Directory
[Symbol(GHS) ]


GHS08,GHS06
[Signal word ]

Danger
[Hazard statements ]

H360-H341-H351-H301
[Precautionary statements ]

P264-P270-P301+P310-P321-P330-P405-P501-P201-P202-P281-P308+P313-P405-P501-P201-P202-P281-P308+P313-P405-P501
[Hazardous Substances Data]

16506-27-7(Hazardous Substances Data)
Hazard InformationBack Directory
[Uses]

Treatment of hematologic cancer, especially non-Hodgkin’s lymphoma.
[Definition]

ChEBI: Bendamustine is a member of benzimidazoles.
[Brand name]

Ribomustine (Amcis AG, Switzerland).
[Enzyme inhibitor]

This nitrogen mustard and anticancer drug (FWfree-acid = 358.26 g/mol; CAS 16506-27-7), also known by its code name SDX-105, its trade names Treanda?, Treakisym?, Ribomustin?, and Levact?, as well as by its systematic name 4-[5-[bis(2-chloroethyl)amino]-1-methylbenzimidazol-2- yl]butanoic acid, is a relatively nonspecific DNA alkylating agent that causes intra- and inter-strand cross-links. Bendamustine is used in the treatment of chronic lymphocytic leukemia (CLL), Hodgkin’s disease, nonHodgkin’s lymphoma, multiple myeloma and lung cancer. Pharmacokinetics: After intravenous infusion, >95% of the drug becomes protein-bound, mainly to albumin; however, only free bendamustine is active. Bendamustine is metabolized by liver cytochrome p450, and elimination (renal) is biphasic, with an initial half-life of 6–10 minutes and a terminal half-life of approximately 30 minutes.
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